Palladium-rich plasmonic nanorattles with enhanced LSPRs via successive galvanic replacement mediated by co-reduction

Abstract

Catalytic transformations under light irradiation have been extensively demonstrated by the excitation of the localized surface plasmon resonances (LSPRs) in noble metal-based nanoparticles. To fully harness the potential of noble metal-based nanocatalysts, it is fundamentally imperative to explore hybrid nano-systems with the most desirable enhanced LSPRs and intrinsic catalytic activities. Pd-containing hollow multimetallic nanostructures transformed from the sacrificial template of Ag via galvanic replacement reaction (GRR) offer such ideal platforms to gain quantitative insights into nanoparticle-catalyzed reactions. In this work, we successfully fabricated Pd-rich plasmonic nanorattles by means of co-reduction mediated GRR using CTAC-stabilized Au@Ag nanocuboids as templates and H₂PdCl₄ as a Pd precursor in the presence of ascorbic acid (AA) acting as a mild reducing agent. Successive titration of Au@Ag nanocuboids with the Pd precursor in the presence of AA modulates the rate of the galvanic replacement reaction as well as effective diffusion of Pd into the Ag matrix, resulting in increased dimensions and enlarged cavity sizes. Reduction of oxidized Ag⁺ back to Ag⁰ by AA, along with the deposition of Pd to form homogeneously mixed bimetallic layers not only prevents LSPRs peak from damping with increasing Pd content but also ensures the enhanced catalytic activities. Through precise control of added H₂PdCl₄ titrant, an unconventional steep increase in extinction intensity accompanied by tunable plasmon resonances shifted towards the NIR spectral region was experimentally observed due to the increasing physical cross-sections and plasmon hybridization in hollow nanorattles. Four colloids of Pd-rich nanorattles obtained by addition of different amounts of the H₂PdCl₄ titrant were used as catalysts for reduction of 4-nitrothiophenol in the presence of NaBH₄ monitored by SERS.